Location: Central Islip, NY (Onsite)
Job Type: Full-Time | Permanent
Shift: 8:30 AM 5:00 PM (may vary)
Industry: Pharmaceutical
Experience Required: 2 to 15 years
Compensation: *,000 *,000
Visa Sponsorship: Not available
Remote Option: No
We are looking for a dedicated Quality Control Chemist to join our team and perform analytical testing in a GMP-regulated laboratory environment. The ideal candidate will have experience in pharmaceutical product testing and familiarity with various analytical instruments and techniques.
Responsibilities:Perform standard and advanced laboratory testing on raw materials, in-process samples, and finished products.
Operate lab instruments such as HPLC, GC, Karl Fischer, ICP, and particle size analyzers.
Ensure compliance with cGMP, data integrity, and good documentation practices.
Support deviation investigations, change control activities, and CAPAs.
Participate in method validations and support production and quality operations.
Maintain accurate and timely documentation in line with regulatory standards.
Execute assigned tasks with attention to detail and in alignment with department protocols.
Collaborate with team members and other departments to meet project deadlines.
Perform other duties as assigned by management.
Bachelor's degree in Chemistry or a related scientific field.
2 15 years of experience in a QC/analytical chemistry role within the pharmaceutical sector.
Strong understanding of lab testing and instrumentation.
Must be able to read, write, and understand scientific materials in English.
Proficiency with MS Office and laboratory software systems.
Comfortable working on-site full-time; no remote options.
Hands-on experience with Inhalation dosage forms (MDI) is a strong advantage.
Background in testing tablets, capsules, liquids, and solids also acceptable.
Prior exposure to GMP, FDA regulatory guidelines, and quality systems.
Experience conducting investigations or root cause analyses.
Work in a controlled laboratory or production area wearing PPE (lab coat, gloves, goggles, etc.).
Ability to lift up to 10 kg and stand or walk for extended periods during an 8-hour shift.
Comfortable using computers and working at a screen for prolonged periods.
Must be willing to work weekday shifts and occasional weekends depending on business needs.
Must be open to working in a pharmaceutical manufacturing environment.
No employment sponsorship or visa support available.
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